KCNJ10 Mutations Disrupt Function in Patients with EAST Syndrome-Reference-Cited by-同舟云学术

KCNJ10 Mutations Disrupt Function in Patients with EAST Syndrome

Published:2011 Issue:3 Volume:119 Page:p40-p48
ISSN:1660-2137
Container-title:Nephron Physiology
language:en
Short-container-title:Nephron Physiol

Author:

Freudenthal Bernard,Kulaveerasingam Duvaraka,Lingappa Lokesh,Shah Mehul A.,Brueton Louise,Wassmer Evangeline,Ognjanovic Milos,Dorison Nathalie,Reichold Markus,Bockenhauer Detlef,Kleta Robert,Zdebik Anselm A.

Publisher

S. Karger AG

Subject

Physiology (medical),Nephrology,General Medicine,Physiology

Reference40 articles.

1. Bartter Syndromes and Other Salt-Losing Tubulopathies

2. Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, andKCNJ10Mutations

3. Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

4. Kir4.1/Kir5.1 channel forms the major K+channel in the basolateral membrane of mouse renal collecting duct principal cells

5. An inward rectifier K+channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4‐Kir5.1 heteromeric channels

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